Non-HFE-related hereditary haemochromatosis, Type 3 (Q97535): Difference between revisions
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A hemocromatose tipo 3 é uma forma de hemocromatose hereditária rara, um grupo de doenças de origem genética caracterizadas pela deposição excessiva de ferro nos tecidos. Assemelha-se à hemocromatose tipo 1 (relacionada ao HFE) e se apresenta com doença hepática, hipogonadismo, artrite, diabetes e pigmentação da pele. | |||
| description / en | description / en | ||
Type 3 hemochromatosis is a form of rare hereditary hemochromatosis, a group of diseases characterised by excessive tissue iron deposition of genetic origin. It resembles type 1 (HFE-related) hemochromatosis and presents with liver disease, hypogonadism, arthritis, diabetes and skin pigmentation. | |||
Revision as of 13:39, 16 August 2026
Type 3 hemochromatosis is a form of rare hereditary hemochromatosis, a group of diseases characterised by excessive tissue iron deposition of genetic origin. It resembles type 1 (HFE-related) hemochromatosis and presents with liver disease, hypogonadism, arthritis, diabetes and skin pigmentation.
| Language | Label | Description | Also known as |
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| default for all languages | ID_506792320 |
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| English | Non-HFE-related hereditary haemochromatosis, Type 3 |
Type 3 hemochromatosis is a form of rare hereditary hemochromatosis, a group of diseases characterised by excessive tissue iron deposition of genetic origin. It resembles type 1 (HFE-related) hemochromatosis and presents with liver disease, hypogonadism, arthritis, diabetes and skin pigmentation. |
